Ikeda Takashi, Sato Ken, Kuwada Naruo, Matsumura Takuya, Yamashita Takuya, Kimura Fumihiko, Hatake Kiyohiko, Ikeda Kazuma, Motoyoshi Kazuo
Third Department of Internal Medicine, National Defense Medical College, Saitama, Japan.
J Leukoc Biol. 2002 Dec;72(6):1198-205.
Interleukin (IL)-4, IL-10, and IL-13 affect monocyte/macrophage functions including regulation of cytokine production. We analyzed the regulatory effects of these cytokines on cytokine production using a human monoblastic cell line, UG3. It is interesting that IL-10 up-regulated, whereas IL-4 and IL-13 down-regulated monocyte chemoattractant protein-1 (MCP-1) production by unstimulated UG3 cells. IL-10-induced expression of MCP-1 mRNA occurred without de novo protein synthesis at transcriptional and post-transcriptional levels. The enhancement of binding activity of nuclear factor Sp1 (Sp-1) and signal transducer and activators of transcription (STAT)1 and 3 but not nuclear factor kappaB (NF-kappaB) was associated with this IL-10-induced MCP-1 expression. Furthermore, IL-10 suppressed lipopolysaccharide (LPS)-induced NF-kappaB binding but not Sp-1. The present results suggest IL-10 has two contrasting actions on the MCP-1 production of monocytes/macrophages, between the resting and activated conditions. The combination of activated Sp-1 and STATs is important for IL-10-induced MCP-1 expression in resting monocytes/macrophages, and the inhibition of LPS-induced NF-kappaB binding is crucial for down-regulation of MCP-1 by IL-10 in stimulated monocytes/macrophages.
白细胞介素(IL)-4、IL-10和IL-13影响单核细胞/巨噬细胞功能,包括细胞因子产生的调节。我们使用人单核母细胞系UG3分析了这些细胞因子对细胞因子产生的调节作用。有趣的是,IL-10上调未受刺激的UG3细胞单核细胞趋化蛋白-1(MCP-1)的产生,而IL-4和IL-13下调其产生。IL-10诱导的MCP-1 mRNA表达在转录和转录后水平均无需从头合成蛋白质即可发生。核因子Sp1(Sp-1)、信号转导子和转录激活子(STAT)1和3而非核因子κB(NF-κB)结合活性的增强与这种IL-10诱导的MCP-1表达相关。此外,IL-10抑制脂多糖(LPS)诱导的NF-κB结合,但不抑制Sp-1。目前的结果表明,IL-10在静息和激活状态下对单核细胞/巨噬细胞的MCP-1产生有两种相反的作用。激活的Sp-1和STATs的组合对于IL-10诱导静息单核细胞/巨噬细胞中MCP-1的表达很重要,而抑制LPS诱导的NF-κB结合对于IL-10下调受刺激单核细胞/巨噬细胞中MCP-1至关重要。